HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012905Generated: October 31, 2026
Hydrochloric Acid → 2,3-Difluoro-4-(4-pentylphenyl)-6-methylbenzaldehyde
https://huagongshe.com/reaction/1012905
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3,4-Difluoro-5-(4-pentylphenyl)toluene | HCID 23118824 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Difluoro-4-(4-pentylphenyl)-6-methylbenzaldehyde | HCID 23118832 | 77.3% |
Reaction Steps
Under a nitrogen atmosphere, 8.93 g of the compound (22) having been dissolved in 66 mL of THF was cooled to −78° C., to which 39.0 mL of sec-BuLi (1 M/L) was added, followed by stirring at the same temperature for 2 hours. 3.56 g of DMF having been dissolved in 44 mL of THF was added thereto, followed by stirring at −78° C. for 1 hour, and after increasing the temperature to room temperature, stirring over night. 20 mL of 3N hydrochloric acid was added thereto, and the aqueous layer was extracted with toluene, which was added to the organic layer. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 7.61 g of 2,3-difluoro-4-(4-pentylphenyl)-6-methylbenzaldehyde (23).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981486B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-2a5939a7c7f74282866803b5cbfeab3f |
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| Source note | uspto-grants-2011_07 |
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